| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:46915722-46916175 | Common:4; Rare:151; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46941329-46941587 | Common:3; Rare:77; Clinvar (benign):1 | ||||
| chr2:47176410-47176590 | Rare:124; Clinvar (benign):5 | ||||
| chr2:48440631-48440867 | Common:7; Rare:114 | ||||
| chr2:53767469-53767903 | Common:5; Rare:141 | ||||
| chr2:53786851-53787184 | Common:1; Rare:125 | ||||
| chr2:53970995-53971152 | Common:5; Rare:71 | ||||
| chr2:54115510-54115700 | Rare:67 | ||||
| chr2:54557908-54557996 | Rare:19 | ||||
| chr2:55050318-55050395 | Rare:29 | ||||
| chr2:55050441-55050763 | Common:4; Rare:96 | ||||
| chr2:55232249-55232726 | Common:3; Rare:134 | ||||
| chr2:55519404-55519757 | Common:1; Rare:100 | ||||
| chr2:58046598-58046875 | Common:2; Rare:88 | ||||
| chr2:58047224-58047305 | Rare:25 |